ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Kdi 792 → [(Z)-5-carboxy-l-pentenyl]-4-(4-chlorophenylsulfonylamino)-1-(3-pyridylmethyl)pyrrolidine hydrochloride

HRID 1488736
ノート
印刷プレビュー

反応式

HRID 1488736 の反応式
Cl.[C:2]([CH2:5][CH2:6][CH2:7]/[CH:8]=[CH:9]\[C@@H:10]1[CH2:14][C@@H:13]([NH:15][S:16]([C:19]2[CH:24]=[CH:23][C:22]([Cl:25])=[CH:21][CH:20]=2)(=[O:18])=[O:17])[CH2:12][N:11]1[CH2:26][C:27]1[CH:28]=[N:29][CH:30]=[CH:31][CH:32]=1)([OH:4])=[O:3]>Cl>[ClH:25].[C:2]([CH2:5][CH2:6][CH2:7]/[CH:8]=[CH:9]\[CH:10]1[CH2:14][CH:13]([NH:15][S:16]([C:19]2[CH:24]=[CH:23][C:22]([Cl:25])=[CH:21][CH:20]=2)(=[O:17])=[O:18])[CH2:12][N:11]1[CH2:26][C:27]1[CH:28]=[N:29][CH:30]=[CH:31][CH:32]=1)([OH:4])=[O:3]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 6442424Kdi 792

生成物 1

HCID 86751375[(Z)-5-carboxy-l-pentenyl]-4-(4-chlorophenylsulfonylamino)-1-(3-pyridylmethyl)pyrrolidine hydrochloride収率 169.1%

試薬・触媒・溶媒 1

HCID 313Hydrochloric Acid溶媒

反応条件

温度
25 °C

実験手順

In 1N-hydrochloric acid (44 ml)-purified water (16 ml) was dissolved crude crystal of (2S,4R)-2-[(Z)-5-carboxy-1-pentenyl]-4-(4-chlorophenylsulfonylamino)-1-(3-pyridylmethyl)pyrrolidine hydrochloride (8.0 g, 0.016 mol) followed by addition of activated carbon (0.8 g) and the mixture was stirred at 25° C. for 1 hour. Then, clarification-filtration was carried out using a 0.25μmembrane prefilter and the filtrate was washed with 1N-hydrochloric acid (4 ml)-purified water (8 ml). While the filtrate was stirred, 1N-aqueous sodium hydroxide solution was added dropwise so as to adjust the solution to pH 2.0 (pH prior to adjustment: 0.4). The mixture was stirred at 20°-25° C. for crystallization and ripening (about 1 hour, pH decreases to 1.51). Then, 1N-aqueous sodium hydroxide solution was added thereto dropwise so as to adjust the solution to pH 2.20. The solution was cooled to 5° C. and 1N aqueous sodium hydroxide solution was added thereto dropwise so as to maintain the solution at pH 2.20. The solution was cooled to 5° C. and 1N-aqueous sodium hydroxide solution was added thereto dropwise so as to maintain the solution at pH 2.20. The solution was then allowed to stand at 0°-5° C. overnight. The next morning the crystal was collected by filtration and washed with cold purified water (8 ml). The washed crystal was dried in vacuo overnight to provide pure crystal (6.77 g) of [(Z)-5-carboxy-l-pentenyl]-4-(4-chlorophenylsulfonylamino)-1-(3-pyridylmethyl)pyrrolidine hydrochloride.

後処理

  1. additionfollowed by addition of activated carbon (0.8 g)
  2. filtrationThen, clarification-filtration
  3. washthe filtrate was washed with 1N-hydrochloric acid (4 ml)-purified water (8 ml)
  4. stirringWhile the filtrate was stirred
  5. addition1N-aqueous sodium hydroxide solution was added dropwise so as
  6. stirringThe mixture was stirred at 20°-25° C. for crystallization
  7. customabout 1 hour
  8. additionThen, 1N-aqueous sodium hydroxide solution was added
  9. temperatureThe solution was cooled to 5° C.
  10. addition1N aqueous sodium hydroxide solution was added
  11. temperaturedropwise so as to maintain the solution at pH 2.20
  12. temperatureThe solution was cooled to 5° C.
  13. addition1N-aqueous sodium hydroxide solution was added
  14. temperaturedropwise so as to maintain the solution at pH 2.20
  15. waitto stand at 0°-5° C. overnight
  16. filtrationThe next morning the crystal was collected by filtration
  17. washwashed
  18. customwith cold purified water (8 ml)
  19. customThe washed crystal was dried in vacuo overnight

出典と根拠

ORDレコード
ord-7b919bc7868d49e6a958202017ac4402
出典データセット
uspto-grants-1997_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05675011

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート